rs74861148
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs74861148(A;A) |
Make rs74861148(A;G) |
Make rs74861148(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 60151311 |
is a | snp |
is | mentioned by |
dbSNP | rs74861148 |
dbSNP (classic) | rs74861148 |
ClinGen | rs74861148 |
ebi | rs74861148 |
HLI | rs74861148 |
Exac | rs74861148 |
Gnomad | rs74861148 |
Varsome | rs74861148 |
LitVar | rs74861148 |
Map | rs74861148 |
PheGenI | rs74861148 |
Biobank | rs74861148 |
1000 genomes | rs74861148 |
hgdp | rs74861148 |
ensembl | rs74861148 |
geneview | rs74861148 |
scholar | rs74861148 |
rs74861148 | |
pharmgkb | rs74861148 |
gwascentral | rs74861148 |
openSNP | rs74861148 |
23andMe | rs74861148 |
SNPshot | rs74861148 |
SNPdbe | rs74861148 |
MSV3d | rs74861148 |
GWAS Ctlg | rs74861148 |
Max Magnitude | 0 |
[PMID 25103139] Common genetic variation in and near the melanocortin 4 receptor gene (MC4R) is associated with body mass index in American Indian adults and children